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SunMark Allergy Relief
SunMark Allergy Relief - 49348-375-10 - (Diphenhydramine Hydrochloride)
Drug Information of SunMark Allergy Relief
| Product NDC: | 49348-375 |
| Proprietary Name: | SunMark Allergy Relief |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SunMark Allergy Relief
| Product NDC: | 49348-375 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030821 |
Package Information of SunMark Allergy Relief
| Package NDC: | 49348-375-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-375-10) > 100 TABLET in 1 BOTTLE |
NDC Information of SunMark Allergy Relief
| NDC Code | 49348-375-10 |
| Proprietary Name | SunMark Allergy Relief |
| Package Description | 1 BOTTLE in 1 CARTON (49348-375-10) > 100 TABLET in 1 BOTTLE |
| Product NDC | 49348-375 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030821 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
